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  Vol. 59 No. 3, March 2002 TABLE OF CONTENTS
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Apolipoprotein E {epsilon}4 Allele and Clinically Defined Vascular Depression

Since this article does not have an abstract, we have provided the first 150 words of the full text and any section headings.

It has been suggested that cerebrovascular disease may favor the development of late-onset depression, and that the particular forms of vascular depression should be individualized.1-2 This suggestion was supported by studies reporting an association between clinically defined vascular risk factors and depression,1 as well as by the frequent occurrence of silent stroke and white matter changes detected by neuroimaging in late-onset depression.2 However, the role of the polymorphism of apolipoprotein E (APOE) in the emergence of vascular depression is still unknown. The APOE{epsilon}4 allele (APOE{epsilon}4) was shown to be a risk factor for Alzheimer disease (AD),3 but the association of this allele with depression4-6 or with cerebrovascular disease7-8 remains controversial. The objective of the present study was, therefore, to clarify the relationship between APOE{epsilon}4 and vascular depression.

Fifty nondemented elderly patients with vascular depression (35 women and 15 men) and 122 controls (74 women . . . [Full Text of this Article]



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